Canonical Allele Identifier: CA2736864408
Gene: SRSF6 HGNC NCBI

Linked Data

dbSNP Id: rs1600861918

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.43460653A>T , CM000682.2:g.43460653A>T GRCh38
NC_000020.10:g.42089293A>T , CM000682.1:g.42089293A>T GRCh37
NC_000020.9:g.41522707A>T NCBI36
NG_029906.1:g.7790A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000244020.5:c.675-50A>T MANE Select ENSP00000244020.3:n.675-50A>T
ENST00000657241.1:c.654+55A>T
ENST00000662078.1:c.674+55A>T ENSP00000499666.1:n.674+55A>T
ENST00000668808.1:c.675-50A>T ENSP00000499517.1:n.675-50A>T
ENST00000670741.1:c.674+55A>T ENSP00000499492.1:n.674+55A>T
ENST00000671022.1:n.765-50A>T
ENST00000244020.4:c.675-50A>T ENSP00000244020.3:n.675-50A>T
ENST00000483871.6:c.*535-50A>T ENSP00000433544.1:n.*535-50A>T
NM_006275.5:c.675-50A>T NP_006266.2:n.675-50A>T
NR_034009.1:n.1113-50A>T
XR_936608.1:n.1434-50A>T
XR_936608.2:n.1434-50A>T
NM_006275.6:c.675-50A>T MANE Select NP_006266.2:n.675-50A>T
NR_034009.2:n.1081-50A>T